A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17137601



Internal ID21451624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31706921..31706921hg38UCSC Ensembl
chr3:31748413..31748413hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg381536
hg191536
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5615793
Supporting Variants
SamplesHG01596
Known GenesOSBPL10, OSBPL10-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17137601
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer